Actively Recruiting

Age: 18Years +
All Genders
ID07007598

Prevention of Post-Polypectomy Colorectal Bleeding by Clips in Patients on Anticoagulants: a Retrospective Single Center Propensity Score Analysis

Led by Helios Kliniken Schwerin · Updated on 2025-06-18

10000

Participants Needed

1

Research Sites

26 weeks

Total Duration

On this page

Sponsors

H

Helios Kliniken Schwerin

Lead Sponsor

M

Medical School Hamburg

Collaborating Sponsor

AI-Summary

What this Trial Is About

This observational study focuses on adults who have undergone colorectal polypectomy and subsequently restarted anticoagulant therapy (excluding acetylsalicylic acid). Researchers aim to find out if applying clips to close the mucosal defect after polypectomy can prevent bleeding in these patients. The study uses a large patient registry from a single center to compare those who received preventive clipping with those who did not. The intervention under evaluation is the endoscopic application of a hemostatic clip after colorectal polypectomy to close the mucosal defect. Participants are grouped based on whether they received at least one prophylactic clip or no clip before restarting anticoagulants. The study is retrospective and observational, analyzing data from over 10,000 colonoscopies to investigate bleeding outcomes. Participants' records are reviewed to assess colorectal bleeding within 30 days after polypectomy. Researchers examine post-procedure outcomes related to bleeding events, considering factors such as polyp size and anticoagulant use. The study does not involve active treatment but monitors and analyzes past patient data to answer its main question about the effectiveness of clips in preventing bleeding after restarting anticoagulants.

CONDITIONS

Brief Title

Prevention of Post-Polypectomy Colorectal Bleeding by Clips in Patients on Anticoagulants

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult who has received a colonoscopy with endoscopic colorectal polypectomy
  • Patient who has received at least one anticoagulant after polypectomy
Not Eligible

You will not qualify if you...

  • Endoscopic polypectomy combined with closure of the mucosal defect by a suturing device or full thickness resection device

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Implementation

Duration - Day of polypectomy

Participants undergo colorectal polypectomy with or without prophylactic clipping to close the mucosal defect after the procedure.

1 procedure visit (in-person)

Monitoring

Duration - Up to 30 days after colorectal endoscopic polypectomy

Participants who have received restarted anticoagulants after polypectomy are observed for post-polypectomy colorectal bleeding.

Follow-up visits as per routine care

Trial Site Locations

Total: 1 location

1

Helios Kliniken Schwerin

Schwerin, Mecklenburg-Vorpommern, Germany, 19055

Actively Recruiting

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Research Team

D

Daniel Schmitz, Dr. med.

M

Martin Kliment

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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Published Research Related To This Trial

Colorectal polypectomy and endoscopic mucosal resection: European Society of Gastrointestinal Endoscopy (ESGE) Guideline - Update 2024.

Monika Ferlitsch, Cesare Hassan, Raf Bisschops...

https://pubmed.ncbi.nlm.nih.gov/38670139